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http://purl.uniprot.org/citations/20101680http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/20101680http://purl.org/dc/terms/identifier"doi:10.1002/ajmg.a.33234"xsd:string
http://purl.uniprot.org/citations/20101680http://purl.uniprot.org/core/author"Tommerup N."xsd:string
http://purl.uniprot.org/citations/20101680http://purl.uniprot.org/core/author"Farooq M."xsd:string
http://purl.uniprot.org/citations/20101680http://purl.uniprot.org/core/author"Kjaer K.W."xsd:string
http://purl.uniprot.org/citations/20101680http://purl.uniprot.org/core/author"Baig S."xsd:string
http://purl.uniprot.org/citations/20101680http://purl.uniprot.org/core/date"2010"xsd:gYear
http://purl.uniprot.org/citations/20101680http://purl.uniprot.org/core/name"Am J Med Genet A"xsd:string
http://purl.uniprot.org/citations/20101680http://purl.uniprot.org/core/pages"495-497"xsd:string
http://purl.uniprot.org/citations/20101680http://purl.uniprot.org/core/title"Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1."xsd:string
http://purl.uniprot.org/citations/20101680http://purl.uniprot.org/core/volume"152A"xsd:string
http://purl.uniprot.org/citations/20101680http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/20101680
http://purl.uniprot.org/citations/20101680http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/20101680
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